Protein modification systems as cancer biomarkers and therapeutic targets
Li Gao1, Yueqin He1, Kexin Wang1
1National Clinical Research Center for Geriatrics and Department of Laboratory Medicine, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Wuhou, Chengdu 610041, China.
Abstract:
Protein post-translational modifications (PTMs), such as acetylation, lactylation, methylation, phosphorylation, ubiquitination, and glycosylation, play central roles in regulating diverse cellular processes, including signal transduction, metabolic adaptation, chromatin organization, and proteostasis. In cancer, PTM networks are extensively rewired, with profound alterations in enzyme levels, protein modification landscapes, and crosstalk among different modification types. These changes collectively shape key cancer hallmarks, such as sustained proliferative signaling, immune evasion, and therapeutic resistance. Recent advances in proteomic technologies have enabled comprehensive mapping of PTM landscapes and their regulatory mechanisms, facilitating the identification of PTM signatures associated with tumor subtyping, disease progression, and treatment response. This review summarized biomarkers and therapeutic targets associated with dysregulated PTM regulatory pathways in cancer.
Insights
Protein post-translational modifications (PTMs) are crucial for cell functions and are altered in cancer, impacting disease progression and treatment. This review covers PTM biomarkers and therapeutic targets in cancer.
Area of Science:
- Biochemistry
- Molecular Biology
- Cancer Research
Background:
- Protein post-translational modifications (PTMs) regulate fundamental cellular processes like signal transduction, metabolism, and proteostasis.
- Dysregulated PTM networks are a hallmark of cancer, influencing sustained proliferation, immune evasion, and therapeutic resistance.
Purpose of the Study:
- To review biomarkers and therapeutic targets associated with altered PTM regulatory pathways in cancer.
- To highlight the role of PTMs in shaping cancer hallmarks and disease progression.
Main Methods:
- Comprehensive literature review of PTMs in cancer.
- Analysis of recent advances in proteomic technologies for PTM mapping.
- Identification of PTM signatures related to tumor characteristics and treatment.
Main Results:
- PTMs, including acetylation, lactylation, methylation, phosphorylation, ubiquitination, and glycosylation, are significantly rewired in cancer.
- Altered PTM enzyme levels and crosstalk contribute to cancer hallmarks.
- PTM signatures can aid in tumor subtyping, predicting progression, and response to therapy.
Conclusions:
- Dysregulated PTMs represent critical areas for cancer biomarker and therapeutic target discovery.
- Understanding PTM networks offers new avenues for cancer treatment strategies.
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